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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/12164
Title: 
Adjuvant therapy with GnRH agonists/tamoxifen in breast cancer should be a good council for patients with hormone receptor-positive tumours and wish to preserve fertility
Other Titles: 
A terapêutica adjuvante com agonista do GnRH/tamoxifeno no cancer de mama pode ser um bom conselho para os pacientes com tumors receptor-hormonal positivos e desejo de preservar a fertilidade
Author(s): 
Institution: 
  • Ctr Human Reprod Prof Franco Jr
  • Paulista Ctr Diag Res & Training
  • Universidade Estadual Paulista (UNESP)
ISSN: 
0306-9877
Abstract: 
Infertility represents one of the main long-term consequences of the chemotherapy used for the adjuvant treatment of breast cancer. Approximately 60-65% of breast cancers express the nuclear hormone receptor in premenopausal women. Adjuvant endocrine therapy is an integral component of care for patients with hormone receptor-positive (HR+) tumours. The GnRH agonist (GnRHa) alone or in combination with tamoxifen produces results at least similar to those obtained with the different chemotherapy protocols in patients with HR+ breast cancer with respect to recurrence-free survival and overall survival. It is time to indicate adjuvant therapy with GnRHa associated with tamoxifen for patients with breast cancer (HR+ tumours) if they want to preserve their reproductive function. The evaluation of ovarian reserve tests: follicle stimulating hormone (FSH), anti-Mullerian hormone (AMH), inhibin B, antral follicle count (AFC) and ovarian volume 6 months, and 1 year after the end of therapy with GnRHa/tamoxifen must be realised. The recurrence-free survival and overall survival should be analysed. The major implication of this hypothesis will be to avoid adjuvant chemotherapy for patients with breast cancer (HR+ tumours) that request fertility preservation. It is expected that ovarian function should not be altered in almost all cases and subsequent pregnancy a real possibility. (C) 2012 Elsevier Ltd. All rights reserved.
Issue Date: 
1-Apr-2012
Citation: 
Medical Hypotheses. Edinburgh: Churchill Livingstone, v. 78, n. 4, p. 442-445, 2012.
Time Duration: 
442-445
Publisher: 
Churchill Livingstone
Source: 
http://dx.doi.org/10.1016/j.mehy.2011.12.015
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/12164
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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